Dopamine D1 and D2 receptors in the fore
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Brice Ongali; Ariel R. Ase; Caroline HΓ©bert; Fatima Amdiss; TomΓ‘s A. Reader
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Article
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2000
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John Wiley and Sons
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English
β 406 KB
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Dystonia musculorum (dt J /dt J ) mutant mice suffer from a degeneration of spinocerebellar tracts as well as a dystrophy of peripheral sensory tracts. This neurological mutant has been proposed as an animal model of human cerebellar ataxia, in particular of the Friedreich's type; thus, it was deeme